Danita currently calls Madison, Alabama, home. She and her husband raise four exceptional children, one of which lives with hereditary angioedema — Ladybug. As a caregiver, Danita hopes that her column will show other caregivers and patients that they’re not alone. Championing the idea to “inform the world,” she seeks to reveal HAE in such a way that even if it’s rare for an individual to have it, it isn’t rare for everyone to know about it.
My screenwriting class sat in stunned silence as they stared at the picture on the screen. Finally, light chuckles filtered through the room. “Whenever you think someone has already done it,” I said to them, “remember this picture.” On…
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